Publications by authors named "Bronwyn Dillon"

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Exome sequencing identifies existing and novel variants in a South African cohort presenting with anterior segment dysgenesis.
Tebogo Marutha, Sue Williams, Michael Novellie, Bronwyn Dillon, Nadia Carstens

Gene· April 2025

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STAC3 disorder: a common cause of congenital hypotonia in Southern African patients.
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker

Eur J Hum Genet· January 2025

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Correction: STAC3 disorder: a common cause of congenital hypotonia in Southern African patients.
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker

Eur J Hum Genet· July 2024

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Mutation analysis and clinical profile of South African patients with Neurofibromatosis type 1 (NF1) phenotype.
Maria Mabyalwa Mudau, Bronwyn Dillon, Clarice Smal, Candice Feben, Engela Honey

Front Genet· March 2024

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Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation.
Bronwyn Dillon, Candice Feben, David Segal, Johannes du Plessis, David Reynders

Mol Genet Genomic Med· August 2020

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